Discover Oncology,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: Oct. 13, 2024
The
aim
of
this
study
was
to
elucidate
the
critical
role
autophagy-related
gene
aggregation
in
gastric
cancer
tumor
microenvironment
cells
and
investigate
their
major
roles
cellular
functions.
In
particular,
expression
these
genes
tumor-associated
fibroblast
subtypes
scrutinized
an
attempt
explain
cell-subpopulation-specific
cell–cell
communication
regulation
study,
single-cell
RNA
sequencing
data
were
first
analyzed
multiple
steps,
including
preprocessing,
cell
clustering,
classification.
Cell
subpopulations
patterns
identified
using
unsupervised
non-negative
matrix
factorization
(NMF)
techniques.
dynamic
aggregates
various
types
deciphered
by
pseudotime
trajectory
analysis
(PTA).
Intercellular
performed
CellChat
R
software
package,
revealing
intricate
exchange
key
signaling
molecules
between
subpopulations,
SCENIC
used
identify
regulatory
networks
reveal
mechanisms
behind
heterogeneity.
associated
with
pan-apoptosis
NMF
decomposition
analysis.
Cell–cell
revealed
subpopulations.
Dynamic
aggregated
pseudotemporal
STAD
observed
PTA.
subtype,
different
ligand-receptor
interactions
immunomodulation
observed.
By
deeply
analyzing
comparing
within
intercellular
communication,
provides
new
insights
into
pan-apoptosis-related
regulating
immune
responses
functions
cancer.
These
findings
pave
way
for
further
exploration
tumorigenesis
regulation,
as
well
laying
foundation
potential
therapeutic
strategies.
Journal of Clinical Medicine,
Journal Year:
2025,
Volume and Issue:
14(2), P. 386 - 386
Published: Jan. 9, 2025
The
blood-brain
barrier
(BBB)
is
a
crucial
structure
that
maintains
brain
homeostasis
by
regulating
the
entry
of
molecules
and
cells
from
bloodstream
into
central
nervous
system
(CNS).
Neurodegenerative
diseases
such
as
Alzheimer's
Parkinson's
disease,
well
ischemic
stroke,
compromise
integrity
BBB.
This
leads
to
increased
permeability
infiltration
harmful
substances,
thereby
accelerating
neurodegeneration.
In
this
review,
we
explore
mechanisms
underlying
BBB
disruption,
including
oxidative
stress,
neuroinflammation,
vascular
dysfunction,
loss
tight
junction
integrity,
in
patients
with
neurodegenerative
diseases.
We
discuss
how
breakdown
contributes
neurotoxicity,
abnormal
accumulation
pathological
proteins,
all
which
exacerbate
neuronal
damage
facilitate
disease
progression.
Furthermore,
potential
therapeutic
strategies
aimed
at
preserving
or
restoring
function,
anti-inflammatory
treatments,
antioxidant
therapies,
approaches
enhance
integrity.
Given
role
neurodegeneration,
maintaining
its
represents
promising
approach
slow
prevent
progression
Frontiers in Neurology,
Journal Year:
2025,
Volume and Issue:
16
Published: Jan. 29, 2025
Alzheimer’s
disease
(AD),
the
leading
cause
of
dementia,
poses
a
growing
global
health
challenge
due
to
an
aging
population.
Early
and
accurate
diagnosis
is
essential
for
optimizing
treatment
management,
yet
traditional
diagnostic
methods
often
fall
short
in
addressing
complexity
AD
pathology.
Recent
advancements
radiomics
artificial
intelligence
(AI)
offer
novel
solutions
by
integrating
quantitative
imaging
features
machine
learning
algorithms
enhance
prognostic
precision.
This
review
explores
application
AI
AD,
focusing
on
key
modalities
such
as
PET
MRI,
well
multimodal
approaches
combining
structural
functional
data.
We
discuss
potential
these
technologies
identify
disease-specific
biomarkers,
predict
progression,
guide
personalized
interventions.
Additionally,
addresses
critical
challenges,
including
data
standardization,
model
interpretability,
integration
into
clinical
workflows.
By
highlighting
current
achievements
identifying
future
directions,
this
article
underscores
transformative
AI-driven
reshaping
diagnostics
care.
Cell Death and Disease,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: Jan. 28, 2025
Abstract
The
understanding
of
neuroimmune
function
has
evolved
from
concepts
immune
privilege
and
protection
to
a
new
stage
interaction.
discovery
skull
meninges
channels
(SMCs)
opened
avenues
for
central
nervous
system
(CNS)
immunity.
Here,
we
characterize
bone
marrow
SMCs
by
detailing
the
anatomical
structures
adjacent
skull,
differences
between
peripheral
marrow,
mainstream
animal
processing
methods,
role
in
monitoring
various
CNS
diseases.
Additionally,
highlight
several
unresolved
issues
based
on
current
research
findings,
aiming
guide
future
directions.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 29, 2025
Alzheimer's
disease
(AD)
is
a
progressive
neurodegenerative
disorder
characterized
by
β-amyloid
(Aβ)
plaques,
neurofibrillary
tangles
(NFTs),
and
neuroinflammation.
Monocytes
macrophages,
particularly
microglia,
play
dual
role
in
AD
pathogenesis.
In
the
early
stages,
they
delay
progression
phagocytosing
Aβ,
but
chronic
activation
leads
to
Aβ
accumulation
exacerbated
Monocyte
chemoattractant
protein
1
(MCP-1)
key
regulator
neuroinflammation,
deposition,
tau
pathology,
making
it
potential
therapeutic
target.
Moreover,
recent
breakthroughs
fluid
imaging
biomarkers
targeted
immunomodulatory
agents
underscore
growing
importance
of
diagnostic
interventions.
This
review
explores
complex
interplay
between
monocytes,
highlighting
their
roles
metabolism,
phosphorylation.
Understanding
these
mechanisms
offers
new
insights
into
developing
effective
strategies
for
AD.
European Journal of Neurology,
Journal Year:
2024,
Volume and Issue:
31(12)
Published: Aug. 20, 2024
Abstract
Background
and
purpose
Peripheral
inflammation
is
probably
involved
in
the
pathogenesis
of
progressive
supranuclear
palsy
(PSP)
it
may
be
a
common
feature
with
Parkinson's
disease
(PD).
The
peripheral
immune
profile
PSP
remains
unclear,
as
well
whether
inflammatory
pathways
differ
from
those
PD.
neutrophil‐to‐lymphocyte
ratio
(NLR)
has
been
proven
to
well‐established
biomarker
systemic
inflammation.
This
study
aimed
evaluate
compared
Methods
A
cross‐sectional
was
conducted
including
patients
PD
healthy
controls
(HCs).
Leukocyte
subpopulations
NLR
were
measured
blood.
Multivariate
linear
regression
post
hoc
tests
applied.
Electronic
databases
searched
November
2023
perform
meta‐analyses
clarify
PSP.
Results
Our
cohort
included
121
PSP,
127
266
HCs.
higher
had
neutrophil
count
Whilst
lower
lymphocyte
found
HCs,
did
not
between
supported
this
profile.
Conclusions
show
an
increased
Different
pathogenic
mechanisms
are
PD,
since
altered
mainly
driven
by
neutrophils.
Understanding
neutrophils'
role
allow
for
development
targeted
therapies.
Ethnopharmacological
relevance:
Pterocarpus
mildbraedii
was
believed
to
have
multiple
benefits,
including
antioxidant,
antipyretic,
antalgic,
anti-convulsant,
and
anxiolytic
effects.
Previous
studies
reported
that
water
extract
(Pm)
contained
secondary
metabolites
able
cross
the
BBB.
However,
Pm's
systemic
mechanism
targets
for
neuroinflammation
remain
largely
unexplored.Aim
of
study:
This
research
used
a
systems
pharmacology
approach
experiment
evaluation
reveal
potential
protective
effects
Pm
against
neuroinflammation,
oxidative
stress,
behavioral
changes
in
an
LPS-induced
Alzheimer's
disease
(AD)
rat
model.Materials
methods:
integrated
network
analysis
experimental
verification
evaluate
pharmacological
PM
AD
systematically.
Swiss
Target
Prediction,
GeneCards,
STRING
databases
were
employed
identify
targets.
The
interaction
between
active
components
hub
confirmed
via
molecular
docking.
GO
KEGG
pathway
analyses
also
carried
out.
Further,
vitro
bioassays
explore
anti-inflammatory
antioxidant
activities
and,
finally,
vivo
neuroinflammatory
stress
markers.Results:
Network
docking
revealed
primarily
regulates
signaling
pathways
such
as
ESR1,
ESR2,
BACE1,
MAPK1,
TLR4,
IL6,
GSK3B
through
like
liquiritigenin
pterocarptriol.
identified
significant
action
AD,
nitrogen
metabolism
VEGF
pathway.
In
vitro,
demonstrated
their
properties,
along
with
inhibitory
on
AchE
BchE.
Behavioral
tests
showed
LPS
exposure
impaired
exploratory
behavior,
spatial
learning,
increased
anxiety
rats,
correlating
brain,
marked
by
elevated
MDA
NO
levels,
decreased
CAT,
SOD,
GSH
levels.
raised
TNF-α
IL-6
levels
while
reducing
dopamine,
serotonin,
AChE
activity.
Notably,
treatment
significantly
mitigated
improved
activity,
restored
neurotransmitter
animals.Conclusion:
paper
established
P.
could
inhibit
its
components,
targets,
pathways.
milbraedii
may
be
candidate
treatment.